Product code KJX— Hematology

JENNER BLOOD STAIN

Classification name
Jenner Stain
Device class
Class 1
Regulation
21 CFR 864.1850
Advisory panel
Hematology
Total cleared
1
First cleared
Most recent

Market context for product code KJX

FDA has cleared 1 device under product code KJX, all in 1984, filed by 1 applicant company. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.

Top applicants under product code KJX

Recent clearances under product code KJX

Data sourced from openFDA. This site is unofficial and independent of the FDA.